rs121913006

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs121913006(A;A)

Make rs121913006(A;G)

Reference

GRCh38 38.1/141

Chromosome

18

Position

31519867

Gene

DSG2

is a	snp
is	mentioned by
dbSNP	rs121913006
dbSNP (classic)	rs121913006
ClinGen	rs121913006
ebi	rs121913006
HLI	rs121913006
Exac	rs121913006
Gnomad	rs121913006
Varsome	rs121913006
LitVar	rs121913006
Map	rs121913006
PheGenI	rs121913006
Biobank	rs121913006
1000 genomes	rs121913006
hgdp	rs121913006
ensembl	rs121913006
geneview	rs121913006
scholar	rs121913006
google	rs121913006
pharmgkb	rs121913006
gwascentral	rs121913006
openSNP	rs121913006
23andMe	rs121913006
SNPshot	rs121913006
SNPdbe	rs121913006
MSV3d	rs121913006
GWAS Ctlg	rs121913006

Max Magnitude

0

OMIM	125671
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121913006(A;A)
Alt	rs121913006(A;A)
Reference	Rs121913006(G;G)
Significance	Pathogenic
Disease	Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy
Variation	info
Gene	DSG2
CLNDBN	Arrhythmogenic right ventricular cardiomyopathy, type 10 not provided Arrhythmogenic right ventricular cardiomyopathy
Reversed	0
HGVS	NC_000018.9:g.29099830G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018303.29, RCV000181198.3, RCV000211715.1,